Lenvatinib enhances antitumor immunity of anti-PD-1 antibody.

IF 2.4 3区 医学 Q3 ONCOLOGY
Yu Kato
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引用次数: 0

Abstract

Lenvatinib is an orally available multi-tyrosine kinase inhibitor that mainly targets vascular endothelial growth factor (VEGF) and fibroblast growth factor (FGF) signaling. These inhibitory activities of lenvatinib exhibit antitumor efficacy, mainly due to their repressive effects on angiogenesis. In addition, a recent non-clinical evaluation using mouse tumor models revealed that lenvatinib causes immunomodulatory effects, including activation of effector T-cells and regulation of tumor-associated macrophages (TAMs). Combined treatment with lenvatinib and anti-programmed cell death-1 antibody (anti-PD-1) resulted in enhanced antitumor activity relative to monotreatment with anti-PD-1 or lenvatinib. This review summarizes the antitumor mechanisms of lenvatinib and of lenvatinib plus anti-PD-1 combination therapy.

Lenvatinib增强抗pd -1抗体的抗肿瘤免疫。
Lenvatinib是一种口服多酪氨酸激酶抑制剂,主要靶向血管内皮生长因子(VEGF)和成纤维细胞生长因子(FGF)信号。lenvatinib的这些抑制活性表现出抗肿瘤功效,主要是由于它们对血管生成的抑制作用。此外,最近一项使用小鼠肿瘤模型的非临床评估显示,lenvatinib可引起免疫调节作用,包括激活效应t细胞和调节肿瘤相关巨噬细胞(tam)。lenvatinib和抗程序性细胞死亡-1抗体(anti-PD-1)联合治疗,相对于抗pd -1或lenvatinib单药治疗,抗肿瘤活性增强。本文就lenvatinib及lenvatinib与抗pd -1联合治疗的抗肿瘤机制进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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